Phase 2 Myeloma Trial, Recruiting NCT07477912 Sponsor: Minsk Scientific-Practical Center for Surgery, Transplantation and Hematology Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT07477912
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older, of any sex.
  • People who are willing and able to give written consent to participate.
  • People who are reasonably physically functional — able to carry out basic daily activities, even if not fully active (assessed using a standard medical scale called ECOG, scores 0 to 2).
  • People diagnosed with multiple myeloma that has come back or stopped responding to treatment, having already received two previous rounds of treatment, and whose myeloma has stopped responding to two specific types of treatment (proteasome inhibitors and immunomodulators).
  • People whose kidneys, liver, and heart are working at an adequate level, as measured by specific blood and imaging tests (confirm with trial site for exact values).
  • People whose blood oxygen levels are adequate and who have little to no breathing difficulty at rest.
  • People with no active graft-versus-host disease (a complication that can occur after certain transplants) at a significant level (Grade 2–4).
  • People whose bone marrow is producing enough blood cells, including white blood cells, lymphocytes, red blood cells, and platelets, at levels meeting specific thresholds (confirm with trial site for exact values).

Who may not be able to join:

  • People who are pregnant or currently breastfeeding.
  • People with a history of, or current, significant neurological conditions such as epilepsy, severe brain injury, dementia, Parkinson's disease, uncontrolled mental illness, psychosis, stroke within the past 3 months, or similar conditions.
  • People whose multiple myeloma has spread to the brain or central nervous system, unless that involvement was effectively treated at least 4 weeks before joining (and at least 8 weeks before the CAR-T cell treatment step) — eligibility in this situation would need to be confirmed with the trial site.
  • People with significant heart disease or a serious heart event that occurred within the past 12 months.
  • People with an active bacterial, viral, or fungal infection requiring treatment, or active or latent hepatitis B, hepatitis C, HIV, HTLV (types 1 or 2), or syphilis.
  • People with a history of autoimmune disease that has damaged an organ or required ongoing immune-suppressing medication within the past 24 months.
  • People with signs of active lung inflammation (pneumonitis) on a recent chest scan, or a history of certain lung conditions including drug-induced pneumonitis, idiopathic pulmonary fibrosis, or organising pneumonia.
  • People with a history of another cancer, unless they have been free of that cancer for at least 24 months (some exceptions apply, such as certain skin cancers, or breast or prostate cancer managed with hormonal therapy — confirm with trial site).
  • People who have recently received certain medications, including high-dose steroids, immune-suppressing drugs, chemotherapy, growth factor injections, live vaccines, certain injections into the spinal fluid, or radiation therapy — specific time restrictions apply for each (confirm with trial site for exact timeframes).
  • People who have previously received treatment targeting a protein called BCMA.
  • People with a known allergy to albumin, DMSO, cyclophosphamide, fludarabine, or tocilizumab.
  • People whom the trial doctor considers unsuitable for any other medical reason.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 8 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Mikhail Uss, MD, State Institution Minsk Scientific and Practical Center for Surgery, Transplantology, and Hematology, Minsk, 220087

Phone: +375291362230

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Minsk Scientific-Practical Center for Surgery, Transplantation and Hematology
Registry
ClinicalTrials.gov
Start date
1 February 2025
Est. completion
1 February 2028

Where this trial is recruiting

Belarus

Primary endpoints

Phase I. Safety; Phase II. Overall response rate

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov